Cencora is looking for a Senior Manager, Medical Devices to lead and deliver regulatory and quality client projects across medical devices, in vitro diagnostics (IVD), and combination products.
Requirements
- University degree in Science, Medicine, Law, Engineering, or a related discipline.
- Significant, hands-on experience in medical device and diagnostics (including IVD) regulatory affairs and quality management.
- Strong analytical and critical-thinking skills, with a track record of resolving complex issues independently and pragmatically.
- Proven project management capability (planning, execution, risk/issue management, and delivery to timelines and quality standards); experience driving change management initiatives is desirable.
- Strong stakeholder management up to client department-head level; excellent written and verbal communication and presentation skills.
- Business-fluent English and local language.
- Companion Diagnostics (CDx) and/or combination products (desired)
Benefits
- Competitive compensation and benefits package
- Senior, highly visible role focused on meaningful client delivery in the medtech space
- Collaborative, expert-led environment where you can share knowledge, influence best practice, and drive continuous improvement
- Professional development opportunities to further deepen your regulatory/quality expertise and leadership capabilities